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Case Reports
. 1990 Jun;149(9):615-7.
doi: 10.1007/BF02034745.

Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency

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Case Reports

Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency

E Schönau et al. Eur J Pediatr. 1990 Jun.

Abstract

Typical features of the "fetal face" or Robinow syndrome are reported in a male infant who presented with ambiguous genitalia and persistence of the Mullerian ducts. Histology of the testes was normal whereas endocrinological studies showed partial deficiency of androgen receptors.

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References

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